Canonical Allele Identifier: PA260249
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7237
ClinVar RCV Id: RCV000007659 RCV000586028 RCV001009487 RCV001375489
ClinVar Variation Id: 35882
ClinVar RCV Id: RCV000029537 RCV000757090 RCV000808411 RCV002256007 RCV004532409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gln1352His
CA260248
NM_000492.4:c.4056G>T
CA325616
NM_000492.4:c.4056G>C